| Strong association of de novo copy number mutations with autism J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ... Science 316 (5823), 445-449, 2007 | 3529 | 2007 |
| Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ... Nature 515 (7526), 209-215, 2014 | 2954 | 2014 |
| Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function DH Skuse, RS James, DVM Bishop, B Coppin, P Dalton, ... Nature 387 (6634), 705-708, 1997 | 971 | 1997 |
| Sex differences in autism spectrum disorder: evidence from a large sample of children and adolescents W Mandy, R Chilvers, U Chowdhury, G Salter, A Seigal, D Skuse Journal of autism and developmental disorders 42, 1304-1313, 2012 | 954 | 2012 |
| Microduplications of 16p11. 2 are associated with schizophrenia SE McCarthy, V Makarov, G Kirov, AM Addington, J McClellan, S Yoon, ... Nature genetics 41 (11), 1223-1227, 2009 | 844 | 2009 |
| Prevalence of feeding problems and oral motor dysfunction in children with cerebral palsy: a community survey S Reilly, D Skuse, X Poblete The Journal of pediatrics 129 (6), 877-882, 1996 | 642 | 1996 |
| Development of sexually abusive behaviour in sexually victimised males: A longitudinal study D Salter, D McMillan, M Richards, T Talbot, J Hodges, A Bentovim, ... The Lancet 361 (9356), 471-476, 2003 | 524 | 2003 |
| Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ... Nature genetics 49 (7), 978-985, 2017 | 506 | 2017 |
| Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ... PLoS genetics 8 (2), e1002521, 2012 | 497 | 2012 |
| Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ... Nature genetics 48 (5), 552-555, 2016 | 453 | 2016 |
| Dopaminergic-neuropeptide interactions in the social brain DH Skuse, L Gallagher Trends in cognitive sciences 13 (1), 27-35, 2009 | 447 | 2009 |
| Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ... Nature communications 6 (1), 8111, 2015 | 446 | 2015 |
| Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism DH Skuse Pediatric research 47 (1), 9-9, 2000 | 428 | 2000 |
| The developmental, dimensional and diagnostic interview (3di): a novel computerized assessment for autism spectrum disorders D Skuse, R Warrington, D Bishop, U Chowdhury, J Lau, W Mandy, ... Journal of the American Academy of Child & Adolescent Psychiatry 43 (5), 548-558, 2004 | 427 | 2004 |
| Avoidance of emotionally arousing stimuli predicts social–perceptual impairment in Asperger's syndrome B Corden, R Chilvers, D Skuse Neuropsychologia 46 (1), 137-147, 2008 | 419 | 2008 |
| Age, gender, and puberty influence the development of facial emotion recognition K Lawrence, R Campbell, D Skuse Frontiers in psychology 6, 761, 2015 | 410 | 2015 |
| Measuring autistic traits: heritability, reliability and validity of the Social and Communication Disorders Checklist DH Skuse, WPL Mandy, J Scourfield The British Journal of Psychiatry 187 (6), 568-572, 2005 | 386 | 2005 |
| Turner syndrome: a cytogenetic and molecular study P Jacobs, P Dalton, R James, K Mosse, M Power, D Robinson, D Skuse Annals of human genetics 61 (6), 471-483, 1997 | 346 | 1997 |
| Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations V Ricotti, WPL Mandy, M Scoto, M Pane, N Deconinck, S Messina, ... Developmental Medicine & Child Neurology 58 (1), 77-84, 2016 | 337 | 2016 |
| X-linked genes and mental functioning DH Skuse Human molecular genetics 14 (suppl_1), R27-R32, 2005 | 288 | 2005 |
Will MandyProfessor in Clinical Psychology, UCL確認したメール アドレス: ucl.ac.uk
